Sevikar 20mg/5mg
Sevikar 20mg/5mg is a medicine authorised by Swissmedic under authorisation number 58778. The authorisation holder is Daiichi Sankyo (Schweiz) AG. The medicinal product code is Synthetic medicines and the dispensing category is B: Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly. First authorisation was granted on 08 October 2008 and the authorisation is valid without a time limit. ATC code C09DB02 places the medicine in the group Agents acting on the renin-angiotensin system.
| Authorisation number | 58778 |
|---|---|
| Name | Sevikar 20mg/5mg |
| Full name | Sevikar 20mg/5mg, Filmtabletten |
| Authorisation holder | Daiichi Sankyo (Schweiz) AG |
| Medicinal product code | Synthetic medicines |
| Dispensing category | B · Prescription only |
| ATC code | C09DB02 |
| First authorisation | 08 October 2008 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Sevikar 20mg/5mg, Filmtabletten | B | 08 October 2008 |
| 2 | Sevikar 40mg/5mg, Filmtabletten | B | 08 October 2008 |
| 3 | Sevikar 40mg/10mg, Filmtabletten | B | 08 October 2008 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 1 | 28 | Tablette(n) | C09DB02 | 02.07.2. | B |
| 2 | 98 | Tablette(n) | C09DB02 | 02.07.2. | B |
| 3 | 28 | Tablette(n) | C09DB02 | 02.07.2. | B |
| 4 | 98 | Tablette(n) | C09DB02 | 02.07.2. | B |
| 5 | 28 | Tablette(n) | C09DB02 | 02.07.2. | B |
| 6 | 98 | Tablette(n) | C09DB02 | 02.07.2. | B |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Sevikar 20mg/5mg authorised in Switzerland?
Yes. Sevikar 20mg/5mg is authorised by Swissmedic under authorisation number 58778, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Sevikar 20mg/5mg have?
Sevikar 20mg/5mg is in dispensing category B. Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly.
Who is the authorisation holder of Sevikar 20mg/5mg?
The authorisation holder is Daiichi Sankyo (Schweiz) AG. The holder carries the legal responsibility for quality, safety and product information of the medicine in Switzerland.
Sources
Swissmedic data as of 01 September 2026. No medical advice. Independent directory, not affiliated with Swissmedic or the FOPH.